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Author Topic: okay, so we went to Seattle for the Evaluation  (Read 3190 times)
breezysummerday
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« on: June 06, 2009, 01:01:15 AM »

1)  Seattle is much more populated then my small town
2)  thank goodness for GPS
3)  need to raise money mostly for my support as a caretaker  (a requirement) during transplantation
     (housing, food...like having a second mortgage)
4)  record breaking temps make me wanna .......wish I was back home.....however the change of
     scenery and dealing with people was exhilarating.
5)  oh yeah, ray passed the evaluation with flying colors!!!
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caregiver to Ray
renal failure 6/08
listed 7/09
~thank you epoman~
Romona
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« Reply #1 on: June 06, 2009, 04:15:31 AM »

Wonderful that Ray passed.  :clap;
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willowtreewren
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My two beautifull granddaughters

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« Reply #2 on: June 06, 2009, 06:20:19 AM »

Yay! :cheer:

Now waiting for more good news.  :clap;
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Wife to Carl, who has PKD.
Mother to Meagan, who has PKD.
Partner for NxStage HD August 2008 - February 2011.
Carl transplanted with cadaveric kidney, February 3, 2011. :)
Wallyz
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« Reply #3 on: June 06, 2009, 08:18:35 AM »

Ack! Next time you come to Seattle, PM so we can meet up.  What center are you guys working with?
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breezysummerday
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« Reply #4 on: June 06, 2009, 01:38:57 PM »

Will keep you in mind Wallyz.
Working with Virginia Mason.
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caregiver to Ray
renal failure 6/08
listed 7/09
~thank you epoman~
okarol
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Photo is Jenna - after Disneyland - 1988

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« Reply #5 on: June 06, 2009, 03:18:15 PM »

What is the average wait time in Seattle?
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Admin for IHateDialysis 2008 - 2014, retired.
Jenna is our daughter, bad bladder damaged her kidneys.
Was on in-center hemodialysis 2003-2007.
7 yr transplant lost due to rejection.
She did PD Sept. 2013 - July 2017
Found a swap living donor using social media, friends, family.
New kidney in a paired donation swap July 26, 2017.
Her story ---> https://www.facebook.com/WantedKidneyDonor
Please watch her video: http://youtu.be/D9ZuVJ_s80Y
Living Donors Rock! http://www.livingdonorsonline.org -
News video: http://www.youtube.com/watch?v=J-7KvgQDWpU
Wallyz
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« Reply #6 on: June 06, 2009, 08:28:22 PM »

Shorter than the national average. I am an A blood type, And I had an SKP offer two months after being listed (At Virginia Mason)  Six months in now, and I am getting offers, but the team is rejecting because the pancreases are bad.

   
Quote
Transplant rate among waitlist patients   0.28   0.19   Statistically Higher (b)      03,04,05,06
Transplant rate (from deceased donors) among waitlist patients   0.20   0.13   Statistically Higher (b)      03,04,05,06
    Mortality rate while on waitlist   0.05   0.07   Not Significantly Different (a)       03,04

So instead of an average 5 year wait (.19/annum transplant rate) it was  a 3 1/2 year wait(.28/annum rate)

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breezysummerday
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« Reply #7 on: June 06, 2009, 11:53:02 PM »



Ray was told a 3 to 4 year wait.  He is O pos.  Ray has 3 sisters that want to test!
(so, maybe sooner then later?  I know, don't hold my breath)
We also got information on how to incorporate ones self so that monetary donations are tax deductible.
It's going to be approximately 200 grand just for the transplant.  However, aftercare is just as an important
factor since we are out of state (alaska, a 3 hour plane ride to seattle).  Housing and nourishment for an estimated
6 weeks after transplantation for 2 people, aye yi yi !! Plus, I need a car.

When the coordinator was discussing with Ray about 'extended criteria transplant', we agreed that 'fresher' is
better.  Kind of a given, actually.  But my reason for bringing this up is that my private thoughts zoomed to one
of Kitkatz's post about 'finding' a small boy with his right kidney outlined on his body.  Reflective of my totally crass
sense of humor fer sure..but I made the coordinater laugh after being so serious about everything and trying to
'suss' us out. 

In the end, I would never have known how to deal with renal failure without this website and all persons that have
shared their story......thank you each and everyone for sharing.  Admins share the same vision as Epoman obviously.

hoping I am in your positive thoughts............ray and deborah 

 
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caregiver to Ray
renal failure 6/08
listed 7/09
~thank you epoman~
kellyt
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« Reply #8 on: June 07, 2009, 04:37:26 AM »

Both you and Ray are in my thoughts.  I didn't find recovery to be too difficult.  My husband didn't stay home with me like we thought he might do.  Once I was home and in my comfty reclyner with my drink and snacks (unsalted, raw almonds) I was great.  Walking was slow and hunched over, but I was able to get around quite nicely.  Hopefully Ray will have the same experience and you all can get home to Alaska quickly.   :)
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1993 diagnosed with glomerulonephritis.
Oct 41, 2007 - Got fistula placed.
Feb 13, 2008 - Activated on "the list".
Nov 5, 2008 - Received living donor transplant from my sister-in-law, Etta.
Nov 5, 2011 - THREE YEARS POST TRANSPLANT!  :D
paris
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« Reply #9 on: June 07, 2009, 09:10:04 AM »

Breezy,  Everything sounds like it is going well.  It also seems like you were very prepared for the meetings.   The money is always a concern, and it shouldn't be.  There is enough stress already!  Let us know when the sisters start the testing.  We'll be praying for a good match and an easy road for all of you.   This is exciting!!     :2thumbsup;
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It's not what you gather, but what you scatter that tells what kind of life you have lived.
breezysummerday
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« Reply #10 on: June 07, 2009, 11:51:22 AM »

     
      :2thumbsup;
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caregiver to Ray
renal failure 6/08
listed 7/09
~thank you epoman~
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